Recent publications:
64. Jake Morrin, Matthew Petitt, and Christopher Abelt*, “1,5-Acrylodan: A Fluorescent Bioconjugate Sensor of Protic Environments,” Organics 2024, 5(4), 493-506; https://doi.org/10.3390/org5040026
63. Orhan Acikgoz* and Christopher Abelt, “Use of Molecular Logic Gates for the Tuning of Chemosensor Dynamic Range,” Molecules 2024, 29(18), 4330; https://doi.org/10.3390/molecules29184330
62. Christopher Abelt*, Ian Day, Junkai Zhao, and Robert Pike, “Fluorescence of Half-Twisted 10-Acyl-1-methyltetrahydrobenzoquinolines,” Molecules 2024, 29(13) 3016; https://doi.org/10.3390/molecules29133016
61. Christopher Abelt* and Kirsten Sweigart, “Twisted 8-Acyl-1-dialkyl-amino-naphthalenes Emit from a Planar Intramolecular Charge Transfer Excited State,” Photochem 2024, 4, 1-13; https://doi.org/10.3390/photochem4010001
60. Hannah J. Naldrett, and Christopher J.Abelt*, “Turn-on fluorescence of a 6-acyl-1-benzoindole by alcohols,” J. Photochem. Photobio. A: Chem. 2022, 432, 114121-141130; https://doi.org/10.1016/j.jphotochem.2022.114121
59. Kristen Lum, Stephanie M. Zielinski, and Christopher J. Abelt*, “Dansyl Emits from a PICT Excited State,” J. Phys. Chem. A 2021, 125, 1229-1233, https://doi.org/10.1021/acs.jpca.0c11229.
58. K. Jacob Blackshaw, Marcus Marracci, Robert T. Korb, Naa-Kwarley Quartey, Annalise K. Ajmani, David J. Hood, Christopher J. Abelt, Belinda I. Ortega, Kate Luong, Andrew S. Petit* and Nathanael M. Kidwell*, “Dynamical signatures from competing, nonadiabatic fragmentation pathways of S-nitrosothiophenol,” Phys. Chem. Chem. Phys. 2020, 22, 12187-12199; https://doi.org/10.1039/ D0CP00941E.
57. Nicholas H. Angello, Robert E. Wiley, Christopher J. Abelt* and Jonathan R. Scheerer*, “Synthesis and Spectrophotometric Analysis of 1-Azafluorenone Derivatives,” Molecules 2020, 25(15), 3358; https://doi.org/10.3390/molecules25153358.
56. Rachel S. Anderson, Newton V. Nagirimadugu, Christopher J. Abelt*, “Fluorescence Quenching of Carbonyl-Twisted 5-Acyl-1-dimethylaminonaphthalenes by Alcohols,” ACS Omega 2019, 4, 14067-14073; https://doi.org/10.1021/acsomega.9b01905.
55. Tao Chen, Samuel W. Lee and Christopher J. Abelt*, "1,5-Prodan Emits from a Planar Intramolecular Charge-Transfer Excited State," ACS Omega 2018, 3, 4816-4823.
54. Isaac G. Alty and Christopher J. Abelt*, "Stereoelectronics of the H-bond-Induced Fluorescence Quenching of 3-Aminofluorenones with Alcohols," J. Phys. Chem. A 2017, 121, 5110-5115.
53. Isaac G. Alty, Douglas W. Cheek, Tao Chen, David B. Smith, Emma Q. Walhout, and Christopher J. Abelt*, “Intramolecular Hydrogen-Bonding Effects on the Fluorescence of PRODAN Derivatives,” J. Phys. Chem. A 2016, 120, 3518–3523.
52. Marisa Daneri, Christopher J. Abelt, “A higher-order preferential solvation model for the fluorescence of two PRODAN derivatives in toluene-alcohol mixtures,” J. Photochem. Photobio. A: Chem. 2015, 310, 106–112.
51. Amy M. Green and Christopher J. Abelt*, "Dual-Sensor Fluorescent Probes of Surfactant-Induced Unfolding of Human Serum Albumin" J. Phys. Chem B. 2015, 119, 3912−3919.
50. Alexandra H. Yoon, Laura C. Whitworth, Joel D. Wagner and Christopher J. Abelt*, "2,5-PRODAN Derivatives as Highly Sensitive Sensors of Low Solvent Acidity," Molecules 2014, 19, 6415-6427.
49. Yuliia Y. Nikitina, Emil S. Iqbal, Hye Joo Yoon, and Christopher J. Abelt* "Preferential Solvation in Carbonyl-Twisted PRODAN Derivatives," J. Phys. Chem. A 2013, 117, 9189–9195.
48. Hannah R. Naughton and Christopher J. Abelt* "Local Solvent Acidities in β-Cyclodextrin Complexes with PRODAN Derivatives," J. Phys. Chem. B 2013, 117, 3323–3327.
47. Amy M. Green, Hannah R. Naughton, Zachariah B. Nealy, Robert D. Pike, and Christopher J. Abelt*, "Carbonyl-Twisted 6-Acyl-2-dialkylaminonaphthalenes as Solvent Acidity Sensors," J. Org. Chem. 2013, 78, 1784–1789.
46. Nicholas A. Lopez and Christopher J. Abelt*, "Synthesis and Properties of Two PRODAN-based Fluorescent Models of Cholesterol," J. Photochem. Photobiol. A: Chemistry, 2012, 238, 35-40.
The remaining publications are found in my CV on the Publications subpage.